• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[腹膜后软组织肉瘤的外科治疗结果]

[Results of surgical therapy of soft tissue sarcoma of the retroperitoneum].

作者信息

Nagel M, Ockert D, Stoelben E, Saeger H D

机构信息

Chirurgische Universitätsklinik Mannheim.

出版信息

Zentralbl Chir. 1994;119(7):488-94.

PMID:7524249
Abstract

Between 1.1.1973 and 30.6. 1993 57 patients underwent operation for soft-tissue sarcoma of the retroperitoneum. The histological classification showed in 21 cases a liposarcoma and in 14 cases a leiomyosarcoma. Other histological types like fibrosarcoma, malignant fibrous histiocytoma or malignant schwannoma were only rarely seen. Complete resection (R-0-resection) was possible in 39 cases (73.5%). 6 patients underwent partial resection (R-2-resection) and 8 patients had only an explorative laparotomy because of an unresectable tumor. To realize a complete resection in 23 cases a multivisceral resection was necessary. The postoperative staging according to AJCC showed for 47.7% of the patients a stage III- or stage IV- disease. The clinical follow-up was observed between 3 months and 14.3 years. The cumulative 5-year-survival-rate for all patients was 38.2%. The most important factor for prognosis was the complete resection, while other factors like sex and age of patients, size of the tumor and histological type did not predict outcome. After complete resection the cumulative 5-year-survival-rate was 46.7%, while after partial resection or explorative laparotomy no patient survived 5 years.

摘要

1973年1月1日至1993年6月30日期间,57例患者接受了腹膜后软组织肉瘤手术。组织学分类显示,21例为脂肪肉瘤,14例为平滑肌肉瘤。其他组织学类型如纤维肉瘤、恶性纤维组织细胞瘤或恶性神经鞘瘤则很少见。39例(73.5%)患者可行根治性切除(R-0切除)。6例患者接受了部分切除(R-2切除),8例患者因肿瘤无法切除仅行了探查性剖腹术。为实现23例患者的根治性切除,需要进行多脏器切除。根据美国癌症联合委员会(AJCC)的术后分期,47.7%的患者为Ⅲ期或Ⅳ期疾病。临床随访时间为3个月至14.3年。所有患者的5年累积生存率为38.2%。预后的最重要因素是根治性切除,而患者的性别、年龄、肿瘤大小和组织学类型等其他因素并不能预测预后。根治性切除后的5年累积生存率为46.7%,而部分切除或探查性剖腹术后无患者存活5年。

相似文献

1
[Results of surgical therapy of soft tissue sarcoma of the retroperitoneum].[腹膜后软组织肉瘤的外科治疗结果]
Zentralbl Chir. 1994;119(7):488-94.
2
Evaluation of a clinically applicable post-surgical classification system for primary retroperitoneal soft-tissue sarcoma.原发性腹膜后软组织肉瘤临床适用术后分类系统的评估
Ann Surg Oncol. 2004 May;11(5):483-90. doi: 10.1245/ASO.2004.09.005. Epub 2004 Apr 12.
3
Caffeine-potentiated chemotherapy and conservative surgery for high-grade soft-tissue sarcoma.咖啡因增强化疗与保肢手术治疗高级别软组织肉瘤
Anticancer Res. 1998 Sep-Oct;18(5B):3651-6.
4
Prognostic factors of retroperitoneal soft tissue sarcomas: analysis of 132 cases.腹膜后软组织肉瘤的预后因素:132例分析
Chin Med J (Engl). 2007 Jun 20;120(12):1047-50.
5
Retroperitoneal sarcoma: 25 years of experience with aggressive surgical treatment at the Institute of Oncology, Ljubljana.腹膜后肉瘤:卢布尔雅那肿瘤研究所25年积极手术治疗经验
J Surg Oncol. 2005 Jul 1;91(1):1-9. doi: 10.1002/jso.20265.
6
Retroperitoneal sarcoma in a series of 51 adults.51例成人腹膜后肉瘤
Eur J Surg Oncol. 1992 Oct;18(5):475-80.
7
[Results of surgical treatment of recurrent retroperitoneal soft tissue sarcomas].[复发性腹膜后软组织肉瘤的外科治疗结果]
Zhonghua Zhong Liu Za Zhi. 1994 Jan;16(1):36-8.
8
Retroperitoneal and truncal sarcomas: prognosis depends upon type not location.腹膜后和躯干肉瘤:预后取决于类型而非位置。
Ann Surg Oncol. 2007 Mar;14(3):1114-22. doi: 10.1245/s10434-006-9255-x. Epub 2007 Jan 7.
9
[Retroperitoneal sarcoma. Treatment of 51 patients].[腹膜后肉瘤。51例患者的治疗]
Harefuah. 1999 Apr 15;136(8):589-93, 660.
10
Retroperitoneal soft-tissue sarcomas: prognosis and treatment of primary and recurrent disease.腹膜后软组织肉瘤:原发性和复发性疾病的预后与治疗
Am Surg. 2000 Sep;66(9):832-6.

引用本文的文献

1
Major vascular resection and prosthetic replacement for retroperitoneal tumors.腹膜后肿瘤的主要血管切除及人工血管置换术。
World J Surg. 2006 Jul;30(7):1344-9. doi: 10.1007/s00268-005-0555-2.